Variant #0000284740 (NC_000001.10:g.1735935T>C, NM_002074.3:c.353A>G (GNB1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1735935T>C
DNA change (hg38) g.1804496T>C
Published as GNB1(NM_002074.3):c.353A>G (p.(Asp118Gly)), GNB1(NM_002074.5):c.353A>G (p.D118G)
ISCN -
DB-ID GNB1_000012 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNB1 NM_002074.3 +?/. - c.353A>G r.(?) p.(Asp118Gly)


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